Canonical Allele Identifier: PA177063
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164412
ClinVar RCV Id: RCV000151318 RCV002281965 RCV002478428 RCV003231344
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Arg1936Trp
CA177061
NM_002473.6:c.5806C>T